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  2. Compatibility (chemical) - Wikipedia

    en.wikipedia.org/wiki/Compatibility_(chemical)

    Such charts are particularly important for polymers [4] as they are often not compatible with common chemical reagents; this may even depend on how the polymers have been processed. [5] For example, 3-D printing polymer tools used for chemical experiments must be chosen to ensure chemical compatibility with care. [6]

  3. Trifluoroacetic acid - Wikipedia

    en.wikipedia.org/wiki/Trifluoroacetic_acid

    Trifluoroacetic acid in a beaker. TFA is the precursor to many other fluorinated compounds such as trifluoroacetic anhydride, trifluoroperacetic acid, and 2,2,2-trifluoroethanol. [4] It is a reagent used in organic synthesis because of a combination of convenient properties: volatility, solubility in organic solvents, and its strength as an ...

  4. Trifluoroacetic anhydride - Wikipedia

    en.wikipedia.org/wiki/Trifluoroacetic_anhydride

    Trifluoroacetic anhydride was originally prepared by the dehydration of trifluoroacetic acid with phosphorus pentoxide. [2] The dehydration might also be carried out with excess α-halogenated acid chlorides. For example, with dichloroacetyl chloride: [3] 2 CF 3 COOH + Cl 2 CHCOCl → (CF 3 CO) 2 O + Cl 2 CHCOOH + HCl

  5. Trifluoroacetyl chloride - Wikipedia

    en.wikipedia.org/wiki/Trifluoroacetyl_chloride

    The compound easily reacts with water and moist air to produce the toxic gas hydrogen chloride and trifluoroacetic acid. [3] [4] Trifluoroacetyl chloride is incompatible with a number of other varieties of chemicals, such as amines, alcohols, alkalis, and strong oxidizers. It reacts strongly with amines and alkalis.

  6. List of reagent testing color charts - Wikipedia

    en.wikipedia.org/wiki/List_of_reagent_testing...

    It is advised to check the references for photos of reaction results. [1] Reagent testers might show the colour of the desired substance while not showing a different colour for a more dangerous additive. [2]

  7. Trifluoroperacetic acid - Wikipedia

    en.wikipedia.org/wiki/Trifluoroperacetic_acid

    Trifluoroperacetic acid (trifluoroperoxyacetic acid, TFPAA) is an organofluorine compound, the peroxy acid analog of trifluoroacetic acid, with the condensed structural formula CF 3 COOOH . [ Note 1 ] It is a strong oxidizing agent for organic oxidation reactions, such as in Baeyer–Villiger oxidations of ketones . [ 1 ]

  8. Drawdown chart - Wikipedia

    en.wikipedia.org/wiki/Drawdown_chart

    Initially the desired coating is applied in a puddle on the drawdown chart. Then the bar is placed at the top of the chart, and drawn down over the paint in order to spread it evenly along the length of the chart. Once this evenly spread paint dries, it can be tested for a variety of properties. [5]

  9. File:Trifluoroacetic acid.svg - Wikipedia

    en.wikipedia.org/wiki/File:Trifluoroacetic_acid.svg

    The following other wikis use this file: Usage on bg.wikipedia.org Трифлуороцетна киселина; Usage on ca.wikipedia.org Àcid trifluoroacètic